S-LIFT Inserter Outer Sleeve Product Usage: The recall
S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is an optional instrument to add further compression of the Inserter into the Implant…
Why was S-LIFT Inserter Outer Sleeve Product Usage: The recalled?
The outer sleeve would not fit over the S-LIFT Inserter assembly because the hole at the top of the sleeve handle was too small.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot/Serial Numbers: 47175
- Product
- S-LIFT Inserter Outer Sleeve Product Usage: The Inserter Sleeve is an optional instrument to add further compression of the Inserter into the Implant…
- Recalling firm
- SpineFrontier, Inc.
- Quantity
- 12 devices
- Distribution
- USA Nationwide Distribution including the states of: FL, TX, OK, MO, NJ, MA
- Recall date
- July 10, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)